Voxel-based morphometry in frontotemporal lobar degeneration with ubiquitin-positive inclusions with and without progranulin mutations. - Wikidata - awgldk - TriplyDB

Voxel-based morphometry in frontotemporal lobar degeneration with ubiquitin-positive inclusions with and without progranulin mutations.

Voxel-based morphometry in frontotemporal lobar degeneration with ubiquitin-positive inclusions with and without progranulin mutations.

http://www.wikidata.org/entity/Q37363779

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Neuroimaging signatures of frontotemporal dementia genetics: C9ORF72, tau, progranulin and sporadics Phenotypic Heterogeneity of Monogenic Frontotemporal Dementia Temporoparietal hypometabolism in frontotemporal lobar degeneration and associated imaging diagnostic errors.ALS and FTLD: two faces of TDP-43 proteinopathy.Neuroanatomy of apathy and disinhibition in frontotemporal lobar degeneration.Concordance and discordance between brain perfusion and atrophy in frontotemporal dementia Alzheimer disease-like phenotype associated with the c.154delA mutation in progranulin.Frontotemporal lobar degeneration: epidemiology, pathophysiology, diagnosis and management.Multimodal FMRI resting-state functional connectivity in granulin mutations: the case of fronto-parietal dementia.Distinct profiles of brain atrophy in frontotemporal lobar degeneration caused by progranulin and tau mutations Imaging correlates of pathology in corticobasal syndrome.TDP-43 subtypes are associated with distinct atrophy patterns in frontotemporal dementia.Does TDP-43 type confer a distinct pattern of atrophy in frontotemporal lobar degeneration?Structural MRI in frontotemporal dementia: comparisons between hippocampal volumetry, tensor-based morphometry and voxel-based morphometry An algorithm for genetic testing of frontotemporal lobar degeneration Clinical and imaging features of Othello's syndrome Prominent phenotypic variability associated with mutations in Progranulin Distinct MRI atrophy patterns in autopsy-proven Alzheimer's disease and frontotemporal lobar degeneration.Frontotemporal lobar degeneration A distinct clinical, neuropsychological and radiological phenotype is associated with progranulin gene mutations in a large UK series Parietal lobe deficits in frontotemporal lobar degeneration caused by a mutation in the progranulin gene Voxel-based morphometry patterns of atrophy in FTLD with mutations in MAPT or PGRN Update on recent molecular and genetic advances in frontotemporal lobar degeneration.FTD and ALS: a tale of two diseases Anterior brain glucose hypometabolism predates dementia in progranulin mutation carriers Distinct anatomical subtypes of the behavioural variant of frontotemporal dementia: a cluster analysis study.Progranulin-associated PiB-negative logopenic primary progressive aphasia.Neuroimaging in frontotemporal lobar degeneration--predicting molecular pathology.Looking for Neuroimaging Markers in Frontotemporal Lobar Degeneration Clinical Trials: A Multi-Voxel Pattern Analysis Study in Granulin Disease.Symmetrical corticobasal syndrome caused by a novel C.314dup progranulin mutation.Subcortical and Deep Cortical Atrophy in Frontotemporal Dementia due to Granulin Mutations.Progranulin: a new avenue towards the understanding and treatment of neurodegenerative disease.Nature versus nurture in frontotemporal lobar degeneration: the interaction of genetic background and education on brain damage.Looking for Measures of Disease Severity in the Frontotemporal Dementia Continuum.Phenotype variability in progranulin mutation carriers: a clinical, neuropsychological, imaging and genetic study.Distinct patterns of brain atrophy in Genetic Frontotemporal Dementia Initiative (GENFI) cohort revealed by visual rating scales.Longitudinal structural gray matter and white matter MRI changes in presymptomatic progranulin mutation carriers.

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Voxel-based morphometry in frontotemporal lobar degeneration with ubiquitin-positive inclusions with and without progranulin mutations.

http://www.wikidata.org/entity/Q37363779

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article científic

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article scientifique

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articolo scientifico

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artigo científico

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bilimsel makale

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scientific article published on March 2007

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vedecký článok

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vetenskaplig artikel

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videnskabelig artikel

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vědecký článek

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name

Voxel-based morphometry in fro ...... without progranulin mutations.

@en

Voxel-based morphometry in fro ...... without progranulin mutations.

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type

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Voxel-based morphometry in fro ...... without progranulin mutations.

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Voxel-based morphometry in fro ...... without progranulin mutations.

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prefLabel

Voxel-based morphometry in fro ...... without progranulin mutations.

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Voxel-based morphometry in fro ...... without progranulin mutations.

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ARCHNEUR.64.3.371

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Voxel-based morphometry in fro ...... without progranulin mutations.

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Bradley F Boeve

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Jennifer Adamson

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Jennifer L Whitwell

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Joseph F Parisi

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Keith A Josephs

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Matthew Baker

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Michael L Hutton

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P2860

Voxel-based morphometry--the methods

Null mutations in progranulin cause ubiquitin-positive frontotemporal dementia linked to chromosome 17q21

Mutations in progranulin cause tau-negative frontotemporal dementia linked to chromosome 17

Frontotemporal lobar degeneration: a consensus on clinical diagnostic criteria

HDDD2 is a familial frontotemporal lobar degeneration with ubiquitin-positive, tau-negative inclusions caused by a missense mutation in the signal peptide of progranulin

Mutations in progranulin are a major cause of ubiquitin-positive frontotemporal lobar degeneration.

Characteristics of frontotemporal dementia patients with a Progranulin mutation.

Corticobasal degeneration and its relationship to progressive supranuclear palsy and frontotemporal dementia.

Structural correlates of early and late onset Alzheimer's disease: voxel based morphometric study

Clinically undetected motor neuron disease in pathologically proven frontotemporal lobar degeneration with motor neuron disease.

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scholarly article

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10.1001/ARCHNEUR.64.3.371

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Rosa Rademakers

Dennis W. Dickson

Ronald C. Petersen

David S Knopman

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2007-03-01T00:00:00Z

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